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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394612생성일: 2026년 10월 24일

Phenol → Thieno(3,2-B)pyridine-2-sulfonic acid (1-(1-amino-isoquinolin-7-ylmethyl)-2-oxo-pyrroldin-3-YL)-amide

https://huagongshe.com/ko/reaction/394612

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Ammonium AcetateHCID 517165—
반응물Thieno[3,2-b]pyridine-2-sulfonic acid[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(s)-yl]-amideHCID 53899839—
생성물Thieno(3,2-B)pyridine-2-sulfonic acid (1-(1-amino-isoquinolin-7-ylmethyl)-2-oxo-pyrroldin-3-YL)-amideHCID 445480—

반응 조건

온도70 °C

반응 단계

Thieno[3,2-b]pyridine-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-amide (1.36 g, 2.88 mmol) and phenol (2.22 g, 23.6 mmol) are melted together with stirring at 70° C. for 5 minutes. Ammonium acetate (2.71 g, 28.8 mmol) is added and the reaction mixture is heated to 90° C. and stirred overnight. Additional ammonium acetate (0.50 g, 5.31 mmol) is added and the reaction is heated for 20 more hours. The reaction is cooled and the residue is purified by RP-HPLC eluting in a gradient of 10% CH3CN/H2O (0.1% TFA) to 100% CH3CN. The appropriate product fractions are lyophilized to provide the title compound as a white solid. The enantiomeric purity is 90.5% ee as determined by analytical Chiralpak AS RP-HPLC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602864B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-4b08a39c19514e579dc74e97f14960ea
출처 메모uspto-grants-2003_08